HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946652Generated: November 2, 2026
Ammonia → Methyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoate
https://huagongshe.com/reaction/1946652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Reactant | Methyl 4-(2-aminothiophene-3-carbonyl)benzoate | HCID 59783735 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 4-(2-(2-aminoacetamido)thiophene-3-carbonyl)benzoate | HCID 59783705 | 28% |
Reaction Steps
In a 100 mL round-bottomed flask was dissolved title compound 491 (1 g, 2.96 mmol) and sodium iodide (0.533 g, 3.55 mmol) in tetrahydrofuran (20 mL) to give a yellow suspension. The mixture was heated at reflux for 2 hours. The mixture was cooled to −78° C. A Dewar-type condenser was attached and filled with dry ice/acetone. Ammonia was introduced as a gas and about 30 mL was condensed into the flask. The reaction mixture was left to warm up to room temperature over the weekend. The solvent was removed in vacuo and the residue was purified via ISCO (50-100% EtOAc/Hexanes; 40 g silica gel column) to obtain product as a tan powder. The solid was purified by suspending it in 1:1 dichloromethane/ether and filtering to afford title compound 492 (265 mg, 28%) as a tan powder which was sufficiently pure for the next step. MS (m/z): 319.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399452B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-823085a3197549a9a36ef48fb574437c |
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| Source note | uspto-grants-2013_03 |
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